Generation of mature myelomonocytic cells through expansion and differentiation of pluripotent stem cell-derived lin-CD34+CD43+CD45+progenitors

a technology of myelomonocytic cells and pluripotent stem cells, which is applied in the direction of cell culture active agents, skeletal/connective tissue cells, embryonic cells, etc., can solve the problems of complex genetic manipulation of bone marrow cells, affecting the study of vitro differentiation studies using human bone marrow cells, and affecting the differentiation effect of myelomonocytic cells. , the cell karyotype is highly abnormal and the functional

Active Publication Date: 2010-04-01
WISCONSIN ALUMNI RES FOUND
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Benefits of technology

[0007]The Examples below disclose a method for efficient generation of mature myelomonocytic cells from hESCs and hiPSCs through expansion of lin−CD34+CD43+CD45+ myeloid-progenitor enriched multipotent hematopoietic cells with granulocyte/macrophage colony stimulating factor (GM-CSF), followed by their directed differentiation toward neutrophil

Problems solved by technology

In vitro differentiation studies using human bone marrow cells are hampered by the limited availability of bone marrow myeloid precursors and the complexity of genetic manipulation of bone marrow cells.
While myeloid leukemia cell

Method used

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  • Generation of mature myelomonocytic cells through expansion and differentiation of pluripotent stem cell-derived lin-CD34+CD43+CD45+progenitors
  • Generation of mature myelomonocytic cells through expansion and differentiation of pluripotent stem cell-derived lin-CD34+CD43+CD45+progenitors
  • Generation of mature myelomonocytic cells through expansion and differentiation of pluripotent stem cell-derived lin-CD34+CD43+CD45+progenitors

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examples

[0050]Basic research into human mature myelomonocytic cell function, myeloid lineage diversification and leukemic transformation, and assessment of myelotoxicity in preclinical drug development requires a constant supply of donor blood or bone marrow samples and laborious purification of mature myeloid cells or progenitors, which are present in very small quantities. To overcome these limitations, we have developed a protocol for efficient generation of neutrophils, eosinophils, macrophages, osteoclasts, DCs, and Langerhans cells from human embryonic stem cells (hESCs). As a first step, we generated lin−CD34+CD43+CD45+ hematopoietic cells highly enriched in myeloid progenitors through coculture of hESCs with OP9 feeder cells. After expansion in the presence of GM-CSF, these cells were directly differentiated with specific cytokine combinations toward mature cells of particular types. Morphologic, phenotypic, molecular, and functional analyses revealed that hESC-derived myelomonocyti...

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Abstract

A method for efficient generation of neutrophils, eosinophils, macrophages, osteoclasts, dendritic cells an Langerhans cells from human embryonic stem cells is disclosed.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This application claims priority from U.S. provisional patent application Ser. No. 61 / 100,313 filed Sep. 26, 2008, and Ser. No. 61 / 194,421 filed Sep. 26, 2008. Both applications are incorporated by reference herein.STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT[0002]This invention was made with United States government support awarded by the following agencies: NIH HL085223, HD044067. The United States government has certain rights in this invention.BACKGROUND OF THE INVENTION[0003]Myeloid cells originate from multipotent hematopoietic stem cells in the bone marrow and consist of granulocytes (neutrophils, eosinophils, basophils) and cells of monocyte / macrophage lineage including dendritic cells (DCs) and osteoclasts. These cells play a critical role in innate and adaptive immunity, inflammatory reactions, and bone remodeling. Transformed myeloid cells give rise to neoplasia, such as acute and chronic myeloid leukemia. Sub...

Claims

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Application Information

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IPC IPC(8): C12N5/00
CPCC12N5/0639C12N2502/1394C12N5/0643C12N5/0645C12N2500/38C12N2500/99C12N2501/15C12N2501/185C12N2501/22C12N2501/23C12N2501/25C12N2506/02C12N2506/45C12N2533/30C12N5/0642C12N2500/90
Inventor SLUKVIN, IGOR I.CHOI, KYUNG-DALVODYANYK, MAKSYM A.
Owner WISCONSIN ALUMNI RES FOUND
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